Canonical Allele Identifier: CA2422829110

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32491320_32491327delinsGGGGTGGT , CM000685.2:g.32491320_32491327delinsGGGGTGGT	GRCh38
NC_000023.10:g.32509437_32509444delinsGGGGTGGT , CM000685.1:g.32509437_32509444delinsGGGGTGGT	GRCh37
NC_000023.9:g.32419358_32419365delinsGGGGTGGT	NCBI36
NG_012232.1:g.853283_853290delinsACCACCCC , LRG_199:g.853283_853290delinsACCACCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682899.1:n.2779_2786delinsACCACCCC
ENST00000683985.1:n.2779_2786delinsACCACCCC
ENST00000357033.9:c.2572_2579delinsACCACCCC MANE Select	ENSP00000354923.3:p.Thr858=
ENST00000357033.8:c.2572_2579delinsACCACCCC	ENSP00000354923.3:p.Thr858=
ENST00000378677.6:c.2560_2567delinsACCACCCC	ENSP00000367948.2:p.Thr854=
ENST00000420596.5:c.94-126128_94-126121delinsACCACCCC	ENSP00000399897.1:n.94-126128_94-126121delinsACCACCCC
ENST00000448370.5:c.94-126617_94-126610delinsACCACCCC	ENSP00000388559.1:n.94-126617_94-126610delinsACCACCCC
ENST00000488902.5:n.336-274264_336-274257delinsACCACCCC
ENST00000619831.4:c.2560_2567delinsACCACCCC	ENSP00000479270.1:p.Thr854=
ENST00000620040.4:c.2572_2579delinsACCACCCC	ENSP00000478150.1:p.Thr858=
NM_000109.3:c.2548_2555delinsACCACCCC	NP_000100.2:p.Thr850=
NM_004006.2:c.2572_2579delinsACCACCCC , LRG_199t1:c.2572_2579delinsACCACCCC	NP_003997.1:p.Thr858=
NM_004009.3:c.2560_2567delinsACCACCCC	NP_004000.1:p.Thr854=
NM_004010.3:c.2203_2210delinsACCACCCC	NP_004001.1:p.Thr735=
XM_006724468.2:c.2572_2579delinsACCACCCC	XP_006724531.1:p.Thr858=
XM_006724469.2:c.2548_2555delinsACCACCCC	XP_006724532.1:p.Thr850=
XM_006724470.2:c.2572_2579delinsACCACCCC	XP_006724533.1:p.Thr858=
XM_006724471.2:c.2572_2579delinsACCACCCC	XP_006724534.1:p.Thr858=
XM_006724472.2:c.2443_2450delinsACCACCCC	XP_006724535.1:p.Thr815=
XM_006724473.2:c.2572_2579delinsACCACCCC	XP_006724536.1:p.Thr858=
XM_006724474.2:c.2572_2579delinsACCACCCC	XP_006724537.1:p.Thr858=
XM_006724475.2:c.2572_2579delinsACCACCCC	XP_006724538.1:p.Thr858=
XM_011545467.1:c.2572_2579delinsACCACCCC	XP_011543769.1:p.Thr858=
XM_011545468.1:c.2572_2579delinsACCACCCC	XP_011543770.1:p.Thr858=
XM_011545469.1:c.2572_2579delinsACCACCCC	XP_011543771.1:p.Thr858=
XM_006724469.3:c.2548_2555delinsACCACCCC	XP_006724532.1:p.Thr850=
XM_006724470.3:c.2572_2579delinsACCACCCC	XP_006724533.1:p.Thr858=
XM_006724474.3:c.2572_2579delinsACCACCCC	XP_006724537.1:p.Thr858=
XM_011545468.2:c.2572_2579delinsACCACCCC	XP_011543770.1:p.Thr858=
XM_017029328.1:c.2572_2579delinsACCACCCC	XP_016884817.1:p.Thr858=
XM_017029329.1:c.2572_2579delinsACCACCCC	XP_016884818.1:p.Thr858=
XM_017029330.2:c.2572_2579delinsACCACCCC	XP_016884819.1:p.Thr858=
NM_000109.4:c.2548_2555delinsACCACCCC	NP_000100.3:p.Thr850=
NM_004006.3:c.2572_2579delinsACCACCCC MANE Select	NP_003997.2:p.Thr858=